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Stochasticity in Signaling Pathways and Gene Regulation: The NFκB Example and the Principle of Stochastic Robustness Marek Kimmel Rice University, Houston, TX, USA
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Credits Rice University –Pawel Paszek –Roberto Bertolusso UTMB – Galveston –Allan Brasier –Bing Tian Politechnika Slaska –Jaroslaw Smieja –Krzysztof Fujarewicz Baylor College of Medicine –Michael Mancini –Adam Szafran –Elizabeth Jones IPPT – Warsaw –Tomasz Lipniacki –Beata Hat
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Gene regulation
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TNF TNF Signaling Pathway Apoptosis Signal NF- B AP-1 Inflammation Proliferation
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Nuclear Factor- B (NF- B) Inducible (cytoplasmic) transcription factor Mediator of acute phase phase reactant transcription (angiotensinogen, SAA) Mediator of cytokine and chemokine expression in pulmonary cytokine cascade Plays role in anti-apoptosis and confering chemotherapy resistance in drug resistant cancers
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IBIB Rel A:NF- B1 nucleus TNF TRAF2/TRADD/RIP TAK/TAB1 IKK Nuclear factor- B (NF- B) Pathway
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Rel A:NF- B1 nucleus 2 Activated IKK NF- B “Activation”
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IK K nucleus TNFR1 Rel A:NF- B1 A20 Negative autoregulation of the NF- B pathway Rel A IBIB IBIB C-Rel NF- B1 NF- B2 RelB Rel A TRAF1 TNF mRNA TTP/Zf36
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Intrinsic sources of stochasticity In bacteria, single-cell level stochasticity is quite well-recognized, since the number of mRNA or even protein of given type, per cell, might be small (1 gene, several mRNA, protein ~10) Eukaryotic cells are much larger (1-2 genes, mRNA ~100, protein ~100,000), so the source of stochasticity is mainly the regulation of gene activity.
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Simplified schematic of gene expression Regulatory proteins change gene status.
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Discrete Stochastic Model Time-continuous Markov chain with state space and transition intensities
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Continuous Approximation only gene on/off discrete stochastic
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Four single cell simulations
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Trajectories projected on (I B ,NF- B n,,time) space, red: 3 single cells, blue: cell population Any single cell trajectory differs from the “averaged” trajectory
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White et al. experiments
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What happens if the number of active receptors is small?
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Low dose responses
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How to find out if on/off transcrition stochasticity plays a role? If on/off rapid enough, its influence on the system is damped Recent photobleaching experiments → TF turnover ~10 sec However, does this quick turnover reflect duration of transcription “bursts”?
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FRAP (Mancini Lab) Fluorescence recovery after photobleaching
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f N B ARE The Model kBkB k dB k dN kNkN
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The Model Fit the model to photobleaching data Obtain estimates of binding constants of the factor Invert binding constants to obtain mean residence times Effect: ~10 seconds
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Estimation of mean times of transcription active/ inactive
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Transcription of the gene occurs in bursts, which are asynchronous in different cells.
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Estimation of mean times of transcription active/ inactive Parameters estimated by fitting the distribution of the level of nuclear message, apparently contradict photobleaching experiments.
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A single gene (one copy) using K-E approximation Amount of protein: Where: and are the constitutive activation and deactivation rates, respectively, is an inducible activation rate due to the action of protein dimers.
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Deterministic description The system has one or two stable equilibrium points depending on the parameters.
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Transient probability density functions Stable deterministic solutions are at 0.07 and 0.63
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Transient probability density functions Stable deterministic solutions are at 0.07 and 0.63
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Transient probability density functions Stable deterministic solutions are at 0.07 and 0.63
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Transient probability density functions Stable deterministic solutions are at 0.07 and 0.63
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Conclusions from modeling Stochastic event of gene activation results in a burst of mRNA molecules, each serving as a template for numerous protein molecules. No single cell behaves like an average cell. Decreasing magnitude of the signal below a threshold value lowers the probability of response but not its amplitude. “Stochastic robustness” allows individual cells to respond differently to the same stimulus, but makes responses well-defined (proliferation vs. apoptopsis).
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References Lipniacki T, Paszek P, Brasier AR, Luxon BA, Kimmel M. Stochastic regulation in early immune response. Biophys J. 2006 Feb 1;90(3):725-42. Paszek P, Lipniacki T, Brasier AR, Tian B, Nowak DE, Kimmel M. Stochastic effects of multiple regulators on expression profiles in eukaryotes. J Theor Biol. 2005 Apr 7;233(3):423-33. Lipniacki T, Paszek P, Brasier AR, Luxon B, Kimmel M. Mathematical model of NF-kappaB regulatory module. J Theor Biol. 2004 May 21;228(2):195-215.
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